ctcRbase

Entry Detail

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General Information

Database ID: SKCM04484 Cancer Type: melanoma Dataset: GSE38495 CTCs/CTM Isolation Method: immunomagnetic purification

Gene Information

ncRNA Symbol: AFG3L2 Full Name: AFG3 like matrix AAA peptidase subunit 2 Category: mRNA Synonyms: SCA28|SPAX5 Chromosome: chr18 Strand: - Coordinate: Start Site(bp): 12328944 End Site(bp): 12377314 Gene Summary: This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008] External Links: Ensembl ID: ENSG00000141385 HGNC ID: HGNC:315 Entrez Gene: 10939

Expression Profile of AFG3L2 Gene

 

Regulatory Relationship

mRNA targets: NA miRNA targets: miRNA Name PITA miRanda RNAhybrid hsa-miR-103a-3p YES YES NO hsa-miR-107 YES YES NO hsa-miR-324-5p YES YES NO hsa-miR-485-5p YES YES NO hsa-miR-488-3p YES YES NO Display: